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Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange

In this work, the limited sensitivity of magnetic resonance is addressed by using the hyperpolarisation method relayed signal amplification by reversible exchange (SABRE-Relay) to transfer latent magnetism from para-hydrogen, a readily isolated spin isomer of hydrogen gas, to components of key plant...

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Autores principales: Alshehri, Adel, Tickner, Ben. J., Iali, Wissam, Duckett, Simon B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510812/
https://www.ncbi.nlm.nih.gov/pubmed/37736655
http://dx.doi.org/10.1039/d3sc03078d
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author Alshehri, Adel
Tickner, Ben. J.
Iali, Wissam
Duckett, Simon B.
author_facet Alshehri, Adel
Tickner, Ben. J.
Iali, Wissam
Duckett, Simon B.
author_sort Alshehri, Adel
collection PubMed
description In this work, the limited sensitivity of magnetic resonance is addressed by using the hyperpolarisation method relayed signal amplification by reversible exchange (SABRE-Relay) to transfer latent magnetism from para-hydrogen, a readily isolated spin isomer of hydrogen gas, to components of key plant oils such as citronellol, geraniol, and nerol. This is achieved via relayed polarisation transfer in which an [Ir(H)(2)(IMes)(NH(2)R)(3)]Cl type complex produces hyperpolarised NH(2)R free in solution, before labile proton exchange between the hyperpolarisation carrier (NH(2)R) and the OH-containing plant oil component generates enhanced NMR signals for the latter. Consequently, up to ca. 200-fold (1)H (0.65% (1)H polarisation) and 800-fold (13)C NMR signal enhancements (0.65% (13)C polarisation) are recorded for these essential oils in seconds. Remarkably, the resulting NMR signals are not only diagnostic, but prove to propagate over large spin systems via a suitable coupling network. A route to optimise the enhancement process by varying the identity of the carrier NH(2)R, and its concentration is demonstrated. In order to prove utility, these pilot measurements are extended to study a much wider range of plant-derived molecules including rhodinol, verbenol, (1R)-endo-(+)-fenchyl alcohol, (−)-carveol, and linalool. Further measurements are then described which demonstrate citronellol and geraniol can be detected in an off-the-shelf healthcare product rose geranium oil at concentrations of just a few tens of μM in single scan (1)H NMR measurements, which are not visible in comparable thermally polarised NMR experiments. This work therefore presents a significant expansion of the types of molecules amenable to hyperpolarisation using para-hydrogen and illustrates a real-world application in the diagnostic detection of low concentration analytes in mixtures.
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spelling pubmed-105108122023-09-21 Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange Alshehri, Adel Tickner, Ben. J. Iali, Wissam Duckett, Simon B. Chem Sci Chemistry In this work, the limited sensitivity of magnetic resonance is addressed by using the hyperpolarisation method relayed signal amplification by reversible exchange (SABRE-Relay) to transfer latent magnetism from para-hydrogen, a readily isolated spin isomer of hydrogen gas, to components of key plant oils such as citronellol, geraniol, and nerol. This is achieved via relayed polarisation transfer in which an [Ir(H)(2)(IMes)(NH(2)R)(3)]Cl type complex produces hyperpolarised NH(2)R free in solution, before labile proton exchange between the hyperpolarisation carrier (NH(2)R) and the OH-containing plant oil component generates enhanced NMR signals for the latter. Consequently, up to ca. 200-fold (1)H (0.65% (1)H polarisation) and 800-fold (13)C NMR signal enhancements (0.65% (13)C polarisation) are recorded for these essential oils in seconds. Remarkably, the resulting NMR signals are not only diagnostic, but prove to propagate over large spin systems via a suitable coupling network. A route to optimise the enhancement process by varying the identity of the carrier NH(2)R, and its concentration is demonstrated. In order to prove utility, these pilot measurements are extended to study a much wider range of plant-derived molecules including rhodinol, verbenol, (1R)-endo-(+)-fenchyl alcohol, (−)-carveol, and linalool. Further measurements are then described which demonstrate citronellol and geraniol can be detected in an off-the-shelf healthcare product rose geranium oil at concentrations of just a few tens of μM in single scan (1)H NMR measurements, which are not visible in comparable thermally polarised NMR experiments. This work therefore presents a significant expansion of the types of molecules amenable to hyperpolarisation using para-hydrogen and illustrates a real-world application in the diagnostic detection of low concentration analytes in mixtures. The Royal Society of Chemistry 2023-08-29 /pmc/articles/PMC10510812/ /pubmed/37736655 http://dx.doi.org/10.1039/d3sc03078d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Alshehri, Adel
Tickner, Ben. J.
Iali, Wissam
Duckett, Simon B.
Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title_full Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title_fullStr Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title_full_unstemmed Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title_short Enhancing the NMR signals of plant oil components using hyperpolarisation relayed via proton exchange
title_sort enhancing the nmr signals of plant oil components using hyperpolarisation relayed via proton exchange
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510812/
https://www.ncbi.nlm.nih.gov/pubmed/37736655
http://dx.doi.org/10.1039/d3sc03078d
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